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Stuart Mossman

Showing results (11-20 of 18) with videos related to

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Acta Oto-Laryngologica|July 18, 2019
Gentamicin vestibulotoxicity with modern systemic dosing regimens: a prospective study using video-oculographyDuncan Smyth, Stuart Mossman, Mark Weatherall, et al.
Annals of the New York Academy of Sciences|September 29, 2011
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosisDavid J Szmulewicz, John A Waterston, Hamish G MacDougall, et al.
Journal of Neurology|December 28, 2012
The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestryRichard H Roxburgh, Renate Marquis-Nicholson, Fern Ashton, et al.
Epilepsia|March 13, 2020
Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsyLynette G Sadleir, Guillem de Valles-Ibáñez, Chontelle King, et al.
The New Zealand Medical Journal|October 9, 2010
Carotid endarterectomy: a Southern North Island regional consensus statementAnnemarei Ranta, Dilip Naik, Pietro Cariga, et al.
Brain : a Journal of Neurology|August 28, 2020
A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder alleleSarah J Beecroft, Andrea Cortese, Roisin Sullivan, et al.
American Journal of Human Genetics|June 25, 2019
Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVASHaloom Rafehi, David J Szmulewicz, Mark F Bennett, et al.
Brain : a Journal of Neurology|February 11, 2020
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansionAndrea Cortese, Stefano Tozza, Wai Yan Yau, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Acta Oto-Laryngologica|July 18, 2019
Gentamicin vestibulotoxicity with modern systemic dosing regimens: a prospective study using video-oculographyDuncan Smyth, Stuart Mossman, Mark Weatherall, et al.
Annals of the New York Academy of Sciences|September 29, 2011
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosisDavid J Szmulewicz, John A Waterston, Hamish G MacDougall, et al.
Journal of Neurology|December 28, 2012
The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestryRichard H Roxburgh, Renate Marquis-Nicholson, Fern Ashton, et al.
Epilepsia|March 13, 2020
Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsyLynette G Sadleir, Guillem de Valles-Ibáñez, Chontelle King, et al.
The New Zealand Medical Journal|October 9, 2010
Carotid endarterectomy: a Southern North Island regional consensus statementAnnemarei Ranta, Dilip Naik, Pietro Cariga, et al.
Brain : a Journal of Neurology|August 28, 2020
A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder alleleSarah J Beecroft, Andrea Cortese, Roisin Sullivan, et al.
American Journal of Human Genetics|June 25, 2019
Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVASHaloom Rafehi, David J Szmulewicz, Mark F Bennett, et al.
Brain : a Journal of Neurology|February 11, 2020
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansionAndrea Cortese, Stefano Tozza, Wai Yan Yau, et al.
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